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1.
Acta Gastroenterol Belg ; 87(1): 40-43, 2024.
Article in English | MEDLINE | ID: mdl-38431790

ABSTRACT

The authors report the case of a 74-years-old woman treated by immunotherapy for a metastatic renal cell carcinoma and having developed an important cholestasis with thrombocytosis, increased CRP, leucocytosis and hypoalbuminemia. Liver remained free of metastases at medical imaging. The diagnosis of a Stauffer syndrome was confirmed by the hepatic biopsy. A complete response of liver disorders was obtained after nephrectomy. From literature survey, Stauffer syndrome should be kept in mind in cancer patients, especially those suffering from a renal cell carcinoma, presenting with cholestasis with no underlying cause.


Subject(s)
Carcinoma, Renal Cell , Cholestasis , Kidney Neoplasms , Liver Diseases , Female , Humans , Aged , Carcinoma, Renal Cell/complications , Carcinoma, Renal Cell/diagnosis , Kidney Neoplasms/complications , Kidney Neoplasms/diagnosis , Kidney Neoplasms/pathology , Syndrome , Liver Diseases/diagnosis , Cholestasis/complications
2.
Acta Gastroenterol Belg ; 85(3): 542, 2022.
Article in English | MEDLINE | ID: mdl-36198302

ABSTRACT

Question: We report the case of a 38y old woman who consulted for chronic diffuse abdominal pain related to previous irritable bowel syndrome diagnosis. Physical examination showed nonblanching reddish hyperpigmented reticular peri-umbilical skin patch (figure 1). What's your diagnosis? Answer: The diagnosis of erythema ab igne was made. Additional investigations confirmed repeated use of hot water bottles applied on abdominal wall for 3 weeks overnight for pain relief. Erythema ab igne is a pathognomonic cutaneous presentation of long-lasting exposure to heat sources (1). The pathophysiology of erythema ab igne remains uncertain. It has been suggested that heat exposure damages dermal vascular plexus and subsequent hemosiderin deposition leading to spider's web-like hyperpigmentation. Differential diagnosis of peri -umbilical dermatological manifestations includes digestive-related entities as caput medusae's sign (related to portal hypertension), Cullen's sign or Walzel's sign (related to acute pancreatitis); and non-digestive-related entities such as livedo reticularis (2). Erythema ab igne is well known from the dermatologists, mostly located on the lower limbs due to prolonged close exposition to heaters or on thighs due to laptop batteries (3). Erythema ab igne is usually of benign course, most often self-resolving after heat exposure discontinuation (3). We believe that it is of paramount to take into consideration the patients' pain and to propose an adapted management to avoid self-treatment.


Subject(s)
Pancreatitis , Spiders , Acute Disease , Animals , Erythema/diagnosis , Erythema/etiology , Hemosiderin , Humans , Pain
3.
Rev Med Liege ; 75(3): 140-144, 2020 Mar.
Article in French | MEDLINE | ID: mdl-32157836

ABSTRACT

Performing endoscopic retrograde cholangiopancreatography (ERCP) in bariatric patients with gastric bypass is often challenging. Many techniques have been described. Recently, Endoscopic ultrasound (EUS) - direct transgastric ERCP (EDGE) by using lumen-apposing metal stent (LAMS) has shown efficacy to reach biliary orifice and perform conventional ERCP with good safety profile and low risk of adverse events.


La réalisation d'une cholangiographie rétrograde (CPRE) chez les patients avec un bypass gastrique a longtemps posé des difficultés. Durant les dernières années, quelques techniques ont été développées pour permettre l'extraction de lithiases cholédociennes chez ces patients. Récemment, une nouvelle technique consistant à créer une fistule gastro-gastrique avec la mise en place d'un stent permettant le passage du duodénoscope a montré un excellent taux de réussite, avec un bon profil de sécurité et un faible taux de complications.


Subject(s)
Choledocholithiasis , Gastric Bypass , Cholangiopancreatography, Endoscopic Retrograde , Choledocholithiasis/surgery , Endosonography , Humans , Stents
4.
Acta Gastroenterol Belg ; 82(1): 43-52, 2019.
Article in English | MEDLINE | ID: mdl-30888753

ABSTRACT

BACKGROUND AND STUDY AIMS: Direct-acting antivirals provide interferon-free treatments for chronic hepatitis C (CHC) virus infection. In Belgium, in 2016, access to these agents was limited to patients with advanced liver fibrosis stages F3 and F4. This study is the first to describe Belgium's patient population ineligible for interferon-free treatment. PATIENTS AND METHODS: This was an observational, cross-sectional, multicentre study that enrolled adult patients with CHC ineligible for interferon-free treatment. Patient data recorded at a single visit included demographic data, disease characteristics, comorbidities, co-medications, treatment status, and laboratory data. RESULTS: Three hundred and three patients from 16 centres in Belgium were included in the statistical analysis. On average, patients were aged 53.5 years and 50.2% were women ; 94.1% had health insurance and 99.0% resided in Belgium. The current hepatitis C virus (HCV) infection was the first infection for 96.0% of patients and the mean time since infection was 20.0 years. Liver fibrosis stage was F0 for 23.7%, F0/F1 or F1 for 38.3%, F1/F2 or F2 for 25.8%, F3 for 7.1%, and F4 for 5.1% of patients ; 28.4% of patients were CHC treatment-experienced. The main reason for ineligibility for interferon-free treatment was lack of reimbursement (84.8%). Other reasons included no treatment urgency or medical decision to wait (27.1%), waiting for future treatment option (8.3%), and no social insurance coverage (3.6%). CONCLUSIONS: This study provides recent data on the CHC patient population and disease characteristics in Belgium that could help medical communities and government agencies manage CHC disease burden.


Subject(s)
Antiviral Agents/therapeutic use , Health Expenditures/statistics & numerical data , Health Services Accessibility , Healthcare Disparities , Hepacivirus , Hepatitis C, Chronic/drug therapy , Universal Health Insurance/statistics & numerical data , Adult , Antiviral Agents/economics , Belgium/epidemiology , Cross-Sectional Studies , Female , Genotype , Hepatitis C, Chronic/epidemiology , Hepatitis C, Chronic/virology , Humans , Liver Cirrhosis/drug therapy , Liver Cirrhosis/epidemiology , Middle Aged , Universal Health Insurance/economics
5.
Pancreatology ; 17(4): 572-579, 2017.
Article in English | MEDLINE | ID: mdl-28600220

ABSTRACT

BACKGROUND/OBJECTIVES: The epidemiology, natural history, complications, and therapeutic management of chronic pancreatitis (CP) are not well described at the national level. This multi-centre prospective observational study involving eight Belgian hospitals aimed to improve the understanding of these aspects of CP in Belgium. METHODS: All patients with a diagnosis of CP based on imaging were eligible for this study. Data were gathered regarding epidemiology, etiology, CP complications, and treatment modalities. RESULTS: A total of 809 patients were included between 1/9/2014 and 31/8/2015. Most patients (794) were adults ≥16-years old, 74% were male, the median age at symptom onset was 47 (38-57) years, the median disease duration was 7 (3-13) years, and the median Izbicki pain score (IPS) was 96 (0-195). The main etiological risk factors according to the TIGAR-O classification were alcohol and tobacco (67%). Current drinkers had lower body mass index (BMI) (21.4 kg/m2 vs 24.1 kg/m2), higher IPS (110 vs 56), and longer inability to work than non-drinkers. Current smokers had lower BMI (21.5 kg/m2 vs 25 kg/m2) and higher IPS (120 vs 30) than non-smokers. Endocrine insufficiency and/or clinical steatorrhea was recorded in 41% and 36% of patients, respectively. The highest IPS was reported in patients with ongoing endotherapy (166 vs 50 for patients who completed endoscopy). CONCLUSION: This multicentric study on CP patients showed that current alcohol drinking and smoking are associated with pain and malnutrition. Pain scores were higher in patients with ongoing endotherapy, independently of surgery.

6.
J Med Virol ; 88(1): 94-9, 2016 Jan.
Article in English | MEDLINE | ID: mdl-26121975

ABSTRACT

No data have been reported yet on treatment outcome in persons who inject drugs (PWID) infected with hepatitis C virus treated with boceprevir or telaprevir in combination with peginterferon (Peg IFN) and ribavirin (RBV). Additionally, there are concerns about the safety of boceprevir and telaprevir in some subgroups of patients with hepatitis C (HCV). In a cohort of HCV patients infected with genotype 1 in Belgium, treatment outcome of patients infected due to IV drug use was analyzed and compared with patients who have no history of substance use. The study population consisted of 179 patients: 78 PWID and 101 controls treated with boceprevir (n = 79) or telaprevir (n = 100) additional to Peg IFN and RBV; 53 (30%) had advanced disease (F3, F4) and 79 (44%) had an antiviral therapy previously. There were no significant differences in the baseline characteristics between both groups, except that PWID patients were more frequently infected with genotype 1a (67% vs 21%), were younger and were predominantly male. Psychiatric complaints during follow-up occurred more frequently in the PWID patients: 24% versus 11% (P = .02). Treatment failure for other reasons than absence of viral response was 70% and 64% in PWID and non-PWID respectively. The sustained viral response (SVR) rates were similar in both groups (71% in PWID vs 72% in non-PWID); with a non-inferiority test with -5% margin there is a difference of -1% (95% CI [-15%, 13%]) and P = 0.30. There are no reasons to exclude PWID from treatment with boceprevir, telaprevir and novel antiviral therapies.


Subject(s)
Antiviral Agents/administration & dosage , Genotype , Hepacivirus/isolation & purification , Hepatitis C, Chronic/drug therapy , Oligopeptides/administration & dosage , Proline/analogs & derivatives , Substance Abuse, Intravenous/complications , Adult , Belgium , Drug Therapy, Combination/methods , Female , Hepacivirus/classification , Hepacivirus/genetics , Hepatitis C, Chronic/virology , Humans , Interferon-alpha/administration & dosage , Male , Middle Aged , Proline/administration & dosage , Prospective Studies , Retrospective Studies , Ribavirin/administration & dosage , Treatment Outcome
7.
Acta Gastroenterol Belg ; 74(2): 277-80, 2011 Jun.
Article in English | MEDLINE | ID: mdl-21861311

ABSTRACT

BACKGROUND AND AIM: Hepatitis C virus genotype 2 is the third in order of frequency in Belgium. The aim of this study was to better define the genotype 2 carriers' epidemiology characteristics. METHODS: In a database comprising 1726 viremic hepatitis C virus patient from the south part of Belgium, the files of 98 genotype 2 carriers were reviewed. RESULTS: There was a strong association between genotype 2 and the mode of transmission. The rate of contamination by invasive medical exams was very high (23%), and statistically different from the one of the others genotypes. Eligibility for antiviral therapies and the rate of sustained viral response were high. CONCLUSION: HCV genotype 2 was highly associated with transmission by invasive medical exams.


Subject(s)
Hepacivirus/genetics , Hepatitis C/diagnosis , RNA, Viral/genetics , Belgium/epidemiology , Female , Genotype , Hepatitis C/epidemiology , Hepatitis C/virology , Humans , Male , Middle Aged , Morbidity/trends , Retrospective Studies , Risk Factors
8.
Acta Gastroenterol Belg ; 74(1): 9-16, 2011 Mar.
Article in English | MEDLINE | ID: mdl-21563648

ABSTRACT

INTRODUCTION: Non-alcoholic Fatty Liver Disease (NAFLD) is increasingly recognised as a source of liver related morbidity and mortality. Hard data on epidemiology and natural history are scarce. AIM: To study demographic and metabolic characteristics of the NAFLD patients seen by Belgian hepatologists. METHODS: Belgian hepatologists filled in a questionnaire for every newly diagnosed NAFLD patient between January 1st and December 31st 2004. Liver biopsy was advised if ALT > 1.5 x ULN and if 3/5 of the criteria for the metabolic syndrome (MS) (ATPI-II) were present, but was not mandatory. Biopsy was scored using the Brunt classification. RESULTS: 230 patients were prospectively included in 9 centres; 54% were males; mean age was 49.4 +/- 13.9 y; mean BMI was 30.6 +/- 4.6 kg/m2. The MS was present in 53%. In 16% formerly undiagnosed diabetes was discovered. 51% had a liver biopsy: 25% met the criteria, 26% did not. Grading did not differ between patients with or without MS. Staging was significantly more severe in patients with MS (2.43 +/- 1.25 vs. 1.73 +/- 1.18, p < 0.001). A subgroup of patients with GGT > 5 x ULN were significantly older (55.9 vs. 47.64 y, p = 0.02), more frequently diabetic (53% vs. 23%, p = 0.01) and had more advanced fibrosis (3.42 vs. 1.08, p = 0.008). ALT levels were variable. CONCLUSIONS: The MS is highly prevalent in Belgian NAFLD patients and is associated with more severe disease. Mild to moderate fibrosis is frequent, and the proposed criteria for liver biopsy are not accurate in selecting these patients. Patients with elevated GGT constitute a subgroup with more advanced disease.


Subject(s)
Alanine Transaminase/blood , Fatty Liver , Liver Cirrhosis , Metabolic Syndrome/epidemiology , Metabolic Syndrome/metabolism , Adolescent , Adult , Aged , Belgium/epidemiology , Cohort Studies , Fatty Liver/epidemiology , Fatty Liver/metabolism , Fatty Liver/pathology , Female , Humans , Liver Cirrhosis/epidemiology , Liver Cirrhosis/metabolism , Liver Cirrhosis/pathology , Male , Middle Aged , Prevalence , Registries/statistics & numerical data , Young Adult
9.
Acta Gastroenterol Belg ; 73(2): 223-8, 2010.
Article in English | MEDLINE | ID: mdl-20690560

ABSTRACT

BACKGROUND/AIMS: A large multicenter trial to compare the efficacy of peginterferon alfa-2a with interferon alfa-2a, in combination with ribavirin, in chronic hepatitis C patients. Efficacy data for prior relapsers are reported because treatment recommendations for this patient population are not well defined. PATIENTS AND METHODS: This study was a multicenter, prospective, randomized clinical trial. The primary efficacy endpoint was sustained virologic response in naive patients (n = 348) and relapsers (n = 95). RESULTS: Sustained virologic response rates were similar in naïve patients and relapsers, both for non-pegylated and pegylated interferon (respectively 27 and 26% and 54 and 43%). Pegylated interferon given for 48 weeks did not improved the relapse rate: 15.9 and 27.3% for non-pegylated and 16.7 and 30.4% for pegylated interferon, naïve vs relapsers respectively. Stepwise logistic regression analysis revealed a significant association between slow response (detectable HCV RNA at week 12 and undetectable at week 24) and relapse in patients with an end-of-treatment response (55% versus 13% respectively; p = 0.02; odds ratio = 6.07). CONCLUSIONS: This trial confirms the value of using peginterferon alfa-2a in both naïve and relapsed patients and provides support for a more tailored approach to treatment for relapsers and particulary for patients with a slow viral response.


Subject(s)
Antiviral Agents/administration & dosage , Hepatitis C, Chronic/drug therapy , Interferon-alpha/administration & dosage , Polyethylene Glycols/administration & dosage , Ribavirin/administration & dosage , Drug Therapy, Combination , Female , Humans , Interferon alpha-2 , Logistic Models , Male , Middle Aged , Prospective Studies , RNA, Viral/analysis , Recombinant Proteins , Treatment Outcome
10.
Acta Gastroenterol Belg ; 73(1): 5-11, 2010.
Article in English | MEDLINE | ID: mdl-20458844

ABSTRACT

BACKGROUND AND STUDY AIMS: Large international clinical trials conducted in the past 5 years rapidly improved the treatment of chronic hepatitis C; however, it is unclear whether the advances seen in clinical trials are being paralleled by similar improvements in routine clinical practice. PegIntrust is a Belgian community-based trial evaluating the sustained virological response. PATIENTS AND METHODS: Observational study of 219 patients receiving pegylated interferon alfa-2b (1.5 microg/kg/wk) and weight-based ribavirin (800-1200 mg/day) for 48 weeks. Primary study end point was sustained virological response (SVR), defined as undetectable HCV RNA 6 months after the completion of treatment. RESULTS: In total, 108 patients (49.3 %) had undetectable HCV RNA at the end of therapy, 91 (41.6%) attaining SVR. Of the 111 patients without an end-of-treatment response, 28 were non-responders, and 21 had virological breakthrough. In total, 134 patients attained early virological response (EVR); 88 (65.7%) of those patients attained SVR. In contrast, 82 (96.5 %) of the 85 patients who did not attain EVR also did not attain SVR. Age, fibrosis score and baseline viral load were identified as important predictors of treatment outcome. The most frequently reported serious adverse events resulting in treatment discontinuation were anemia (n = 10), fatigue/asthenia/malaise (n = 6) and fever (n = 3). CONCLUSION: Our data indicate that treatment of chronic hepatitis C with PEG-IFN alfa-2b plus weight-based ribavirin results in favourable treatment outcomes in a Belgian cohort of patients treated in community-based clinical practice.


Subject(s)
Antiviral Agents/administration & dosage , Hepatitis C, Chronic/drug therapy , Interferon-alpha/administration & dosage , Polyethylene Glycols/administration & dosage , Ribavirin/administration & dosage , Adult , Belgium , Cohort Studies , Drug Therapy, Combination , Female , Humans , Interferon alpha-2 , Male , Middle Aged , Recombinant Proteins , Treatment Outcome
12.
Acta Gastroenterol Belg ; 69(2): 203-8, 2006.
Article in English | MEDLINE | ID: mdl-16929616

ABSTRACT

UNLABELLED: Frequency of atypical symptoms in patients suffering from gastro-oesophageal reflux disease (GORD) is not well known, and the optimal management of such symptoms has not been well established. Our aims were to set up an observatory of these atypical symptoms of GORD in Belgium and to study the efficacy of one month treatment with esomeprazole 40 mg. PATIENTS AND METHODS: Gastroenterologists participating in this observational survey were asked to register every new outpatient with symptoms of GORD during a period of 20 consecutive working days. All patients who reported predominant presence of atypical manifestations of GORD were documented and characterized more in detail. In patients with dominant chest pain or ENT symptoms, a treatment with esomeprazole 40 mg daily during 4 weeks was proposed. RESULTS: 90 gastroenterologists included 2864 patients consulting for symptoms suggestive of GORD, including 776 (27.1%) with dominant atypical symptoms. Endoscopy (performed in 2800 patients) showed significantly less oesophagitis in atypical than in typical GORD patients (68% vs. 81.1%; P < 0.0001). Management of atypical GORD patients appeared to be very heterogeneous. Overall 516/776 patients were included in the open phase of treatment with esomeprazole 40 mg, but data for analysis are only available in 228 patients. After one month, symptoms had disappeared in 57.1% and significantly improved in 26.6%. CONCLUSION: Atypical GORD represents a large number of consultations in gastroenterology in Belgium. It is associated with less endoscopic lesions than typical GORD. Its management is heterogeneous reflecting the lack of guidelines on this topic. Response rate after esomeprazole 40 mg for one month in this open uncontrolled trial was high. This result warrants confirmation in a placebo-controlled trial.


Subject(s)
Anti-Ulcer Agents/therapeutic use , Enzyme Inhibitors/therapeutic use , Esomeprazole/therapeutic use , Gastroesophageal Reflux/drug therapy , Gastroesophageal Reflux/epidemiology , Adolescent , Adult , Aged , Aged, 80 and over , Anti-Ulcer Agents/administration & dosage , Belgium/epidemiology , Child , Dose-Response Relationship, Drug , Endoscopy, Gastrointestinal , Enzyme Inhibitors/administration & dosage , Esomeprazole/administration & dosage , Female , Gastroesophageal Reflux/diagnosis , Humans , Male , Middle Aged , Proton Pump Inhibitors , Proton Pumps/administration & dosage , Treatment Outcome
13.
Aliment Pharmacol Ther ; 20(1): 15-22, 2004 Jul 01.
Article in English | MEDLINE | ID: mdl-15225166

ABSTRACT

AIM: To evaluate the efficacy of early interferon alpha-2b in non-post-transfusion acute hepatitis C virus: a prospective study with historical comparison. PATIENTS: Group A: 28 patients prospectively treated for acute hepatitis C virus with daily regimen of interferon 5 million units for 2 months. Group B: historical series of 16 patients with untreated acute hepatitis C virus. RESULTS: There was no significant difference between the two groups with regard to gender, age, icterus, alanine aminotransferase, or genotypes. In group B, hepatitis spontaneously resolved in three of 16 (19%) patients (follow-up 1-7 years). In group A, 21 of 25 patients became sustained viral responders (75%; P = 0.0003 vs. group B). Factors include not predictive of sustained viral response: age, gender, sources of infection, presence of icterus, alanine aminotransferase peak, bilirubin peak, incubation period, presence of hepatitis C virus antibodies at presentation, or genotypes. The time from presentation to the start of therapy was, however, significantly shorter in sustained viral responders (43 +/- 31 days) than in relapsers or non-responders (88 +/- 52 days) (P = 0.016). CONCLUSIONS: Early treatment of acute hepatitis C virus with interferon prevents chronicity. A short waiting time from presentation to treatment appears as the most relevant predictive factor for sustained response.


Subject(s)
Antiviral Agents/therapeutic use , Hepatitis C/drug therapy , Interferon-alpha/therapeutic use , Acute Disease , Adolescent , Adult , Female , Humans , Interferon alpha-2 , Male , Middle Aged , Prospective Studies , Recombinant Proteins , Remission, Spontaneous , Risk Factors , Treatment Outcome , Viral Load
14.
J Viral Hepat ; 10(6): 460-6, 2003 Nov.
Article in English | MEDLINE | ID: mdl-14633181

ABSTRACT

The standard treatment for patients with chronic hepatitis C is a 6-12-month combination therapy with interferon alpha and ribavirin. Induction treatment could result in a faster early decline of the hepatitis C virus (HCV) load and a better response rate. Naive chronically infected HCV patients (n = 454) were randomized into two arms to receive either induction treatment with interferon alpha 2b 5 million units (MU) subcutaneously (s.c.) daily during a period of 8 weeks (arm A); or treatment with interferon alpha 2b 5 MU s.c. three times a week (TIW) for a period of 8 weeks (arm B). After week 8, interferon treatment in both arms was 3 MU s.c. TIW for a total period of 12 months. In both arms, ribavirin (1000-1200 mg orally per day) was added at week 4. Induction treatment resulted in a higher virological response at week 8 of treatment (66%vs 47%; P < 0.01). However, response at the end of treatment and at 6 months follow-up was not different (53%vs 50%, 41%vs 33%). The occurrence of adverse events and the drop-out rate were similar in both arms. Although an early virological response is observed more frequently in the induction treatment, end of treatment response and sustained responses did not differ.


Subject(s)
Hepatitis C, Chronic/drug therapy , Interferon-alpha/administration & dosage , Interferon-alpha/therapeutic use , Ribavirin/administration & dosage , Ribavirin/therapeutic use , Adolescent , Adult , Aged , Alanine Transaminase/blood , Antiviral Agents/administration & dosage , Antiviral Agents/pharmacology , Antiviral Agents/therapeutic use , Belgium , Drug Therapy, Combination , Genotype , Hepatitis C, Chronic/diagnosis , Hepatitis C, Chronic/virology , Humans , Interferon alpha-2 , Interferon-alpha/pharmacology , Liver Cirrhosis , Middle Aged , Netherlands , RNA, Viral/blood , Recombinant Proteins , Ribavirin/pharmacology , Viral Load
15.
Obes Surg ; 11(4): 524-7, 2001 Aug.
Article in English | MEDLINE | ID: mdl-11501368

ABSTRACT

BACKGROUND: The authors have been using the new saline-filled BioEnterics intragastric balloon (BIB) since 1995. METHODS: By now, more than 650 BIBs have been implanted on our Unit. RESULTS: Because of close collaboration between the engineers and the users, and after several modifications, an easy-to-use balloon is available. In addition, we have developed 3 instruments which provide easy and quick removal of the BIB. CONCLUSION: The device, supported by a competent motivated team, is another modality available for weight loss.


Subject(s)
Catheterization/instrumentation , Catheterization/methods , Gastric Balloon , Anesthesia, General/methods , Catheterization/adverse effects , Equipment Design , Equipment Failure , Gastric Balloon/adverse effects , Gastric Balloon/standards , Humans , Patient Care Team , Risk Factors , Treatment Outcome , Weight Loss
16.
Rev Med Liege ; 56(1): 25-30, 2001 Jan.
Article in French | MEDLINE | ID: mdl-11256133

ABSTRACT

Between April 1998 and July 1999, we prospectively investigated 152 patients with gastric or duodenal ulcer and we observed concomitant H. pylori infection in 72.8% and 78.5% respectively. We proposed to the GPs of these patients the recommended triple therapy (omeprazole 20 mg, amoxicillin 1 g and clarithromycin 500 mg (OAC) twice daily for 7 or 10 days). H. pylori eradication was tested using the C13-urea breath test. Our results showed a modest overall eradication rate of about 70%. We have to persuade the patients and the GPs of the benefit of antibiotics and of the importance of the correct dosages. We have to continue to follow the resistance against antibiotics.


Subject(s)
Helicobacter Infections/drug therapy , Helicobacter Infections/epidemiology , Helicobacter pylori , Peptic Ulcer/microbiology , Adult , Aged , Aged, 80 and over , Amoxicillin/therapeutic use , Anti-Bacterial Agents/therapeutic use , Anti-Ulcer Agents/therapeutic use , Belgium/epidemiology , Clarithromycin/therapeutic use , Drug Therapy, Combination , Female , Helicobacter Infections/complications , Humans , Male , Middle Aged , Omeprazole/therapeutic use , Penicillins/therapeutic use , Prevalence , Prospective Studies , Treatment Outcome , Urban Population/statistics & numerical data
17.
JBR-BTR ; 84(6): 258-61, 2001.
Article in French | MEDLINE | ID: mdl-11822367

ABSTRACT

In our institution, MRCP is actually replacing diagnostic ERCP. This study is addressing its accuracy in the diagnosis of symptomatic choledocholithiasis. 137 MRCP were performed in patients with upper abdominal pain and biological anomalies (n = 48), pain with cholelithiasis at sonography (n = 69) or non-alcoholic acute pancreatitis (n = 20) on a 1.5 T system with high gradients using a standardized combination of breath-hold HASTE and RARE sequences. We included in our study 74 patients who underwent as second test ERCP (n = 36), peroperative cholangiography (n = 13), or extensive follow-up with laboratory tests and/or sonography (n = 25). All examinations were judged as diagnostic, discrepancies between direct cholangiography and MRCP being noted in 4 patients (5.4%). Lithiasis was misinterpreted on MRCP as bubbles in 2 patients after sphincterotomy or surgery. We had two false positive diagnoses on MRCP: in one patient peroperative cholangiography was negative and in the other one ERCP was negative. With a sensitivity and PPV of 92%, a specificity and NPV of 96% MRCP in our experience is shown as an accurate diagnostic tool for the detection of stone in the common bile duct replacing ERCP.


Subject(s)
Cholangiography , Gallstones/diagnosis , Image Enhancement , Magnetic Resonance Imaging , Adolescent , Adult , Aged , Aged, 80 and over , Cholangiopancreatography, Endoscopic Retrograde , Female , Humans , Male , Middle Aged
18.
Rev Med Liege ; 55(2): 74-5, 2000 Feb.
Article in French | MEDLINE | ID: mdl-10769572

ABSTRACT

The incidence of pancreatic cancer (PC) is increasing in developing countries. Smoking, reduced consumption of fruits and vegetables, chronic pancreatitis appear to be the best established risk factors. PC is often diagnosed at a late stage. We have to look for it when dyspepsia with weight loss, pancreatic pain or impaired glucose tolerance occurs. Tumor markers are briefly exposed and we discuss the place of endoscopic retrograde cholangiopancreatography (ERCP) after non invasive imaging techniques.


Subject(s)
Biomarkers, Tumor/analysis , Cholangiopancreatography, Endoscopic Retrograde , Pancreatic Neoplasms , Diagnosis, Differential , Diet , Glucose/metabolism , Humans , Incidence , Pain/etiology , Pancreatic Neoplasms/diagnosis , Pancreatic Neoplasms/epidemiology , Pancreatic Neoplasms/pathology , Risk Factors , Smoking/adverse effects , Weight Loss
19.
Rev Med Liege ; 55(2): 76-83, 2000 Feb.
Article in French | MEDLINE | ID: mdl-10769573

ABSTRACT

Accurate preoperative staging is now more prerequisite in the management of cancer of the pancreas and ampulla in order to orientate the patient toward the best selected treatment: either a curative or a palliative surgery associated or not with a pre- or postoperative multimodal therapy, or an endoscopic palliative technique which does not require surgery. Endoscopic ultrasonography (EUS) appears to be a highly accurate diagnostic procedure in the assessment of local resectability because it enables detailed visualization of the pancreatic gland, the depth of infiltration into the surrounding tissue and organs and visualisation of regional lymph nodes involvement. EUS-guided fine needle aspiration for cytology will provide a tissue diagnosis. The likelihood of successful resection for palliative or cure can be predicted before surgery. The following overview will point out the clinical impact of EUS on diagnosis, staging and management of these tumors.


Subject(s)
Ampulla of Vater/diagnostic imaging , Common Bile Duct Neoplasms/diagnostic imaging , Endosonography/methods , Pancreatic Neoplasms/diagnostic imaging , Ampulla of Vater/pathology , Ampulla of Vater/surgery , Common Bile Duct Neoplasms/pathology , Common Bile Duct Neoplasms/surgery , Diagnosis, Differential , Humans , Palliative Care , Pancreatic Neoplasms/pathology , Pancreatic Neoplasms/surgery , Prognosis
20.
Rev Med Liege ; 53(4): 193-8, 1998 Apr.
Article in French | MEDLINE | ID: mdl-9641013

ABSTRACT

Sphincter of Oddi dysfunction (SOD) is an obstructive syndrome of the papilla not resulting from a stone. It may cause recurrent biliary type pain to cholecystectomized patients. SOD is caused by sphincter dyskinesia or benign stenosis. Diagnosis is usually based on symptoms, serum biochemistry, endoscopic retrograde cholangiopancreatography and Sphincter of Oddi manometry. The latter is the best means of evaluating Sphincter of Oddi dynamics. However, because of the many inconveniences of Sphincter of Oddi manometry and of its high morbidity rate, it is seldom used. Non invasive techniques, such as cholescintigraphy, have been developed to replace Sphincter of Oddi manometry in diagnosing SOD. Patients can be cured by sphincterotomy. Certain drugs could also be effective but few controlled studies have been carried out of date.


Subject(s)
Cholecystectomy , Sphincter of Oddi/physiopathology , Biliary Tract Diseases/etiology , Cholangiopancreatography, Endoscopic Retrograde , Colic/etiology , Common Bile Duct Diseases/complications , Common Bile Duct Diseases/diagnosis , Common Bile Duct Diseases/physiopathology , Common Bile Duct Diseases/therapy , Constriction, Pathologic/physiopathology , Humans , Manometry , Pressure , Recurrence , Sphincter of Oddi/surgery , Sphincterotomy, Endoscopic
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